Plastic Heart Tubes with Chocolate Lentils
Reason Bee International is recalling Plastic Heart Tubes with Chocolate Lentils because they may contain undeclared milk protein.
Candy Sweet Spots recall
Recalled by Bee International, Inc. · Chula Vista, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Candy Sweet Spots, 2oz. (3 display packages/case; 12-2oz packages/display case). UPC 0-73563-00471-6
Quantity: 4481 cases
Food: Chocolate & candy
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Mfg code: 2158613 (Date of manufacture: 158 day of 2012) Mfg code: 2335613 (Date of manufacture: 335 day of 2012)
Where it was sold
Nationwide.
FDA's distribution note: Nationwide in US and Canada.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Bee International, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 12, 2013
- In FDA report of
- Jan 22, 2014
- Terminated
- May 13, 2014
- FDA recall number
- F-1403-2014 · event 67077
- Official record
- FDA enforcement report search
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